Georg F Hoffmann's Books

The Encyclopaedia Logic, with the Zustze

Part I of the Encyclopaedia of Philosophical Sciences with the Zusätze

By: Georg Wilhelm Friedrich Hegel

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The Encyclopaedia Logic, with the Zustze

Part I of the Encyclopaedia of Philosophical Sciences with the Zusätze

By: Georg Wilhelm Friedrich Hegel

The appearance of this translation is a major event in English-language Hegel studies, for it is more than simply a replacement for Wallace's translation cum paraphrase. Hegel's Prefaces to each of the three editions of the Enzyklopädie are translated for the first time into English. There is a very detailed Introduction translating Hegel's German, which serves not only as a guide to the translator's usage but also to Hegel's. Also included are a detailed bilingual annotated glossary, very extensive bibliographic and interpretive notes to Hegel's text (28 pp.), an Index of References for works cited in the notes, a select Bibliography of recent works on Hegel's logic, and a detailed Index (16 pp.). The translation is guided by the (correct) principle that rendering Hegel's logical thought clearly and consistently requires rendering his technical terms logically. . . . This ought immediately to become the standard translation of this important work. --Kenneth R. Westphal, in Review of Metaphysics

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Page Count

438

Publisher

Hackett Publishing

Published Date

ISBN 10

0872200701

ISBN 13

9780872200708

Atlas of Inherited Metabolic Diseases

By: William L Nyhan,Georg F Hoffmann

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Atlas of Inherited Metabolic Diseases

By: William L Nyhan,Georg F Hoffmann

In a field where even experts may find that years have elapsed since they last encountered a child with a given disorder, it is essential for the clinician to have a comprehensive source of practical and highly illustrated information covering the whole spectrum of metabolic disease to refer to. The content is divided into sections of related disorders, including disorders of amino acid metabolism, lipid storage disorders, and mitochondrial diseases for ease of reference, with an introductory outline where appropriate summarizing the biochemical features and general management issues. Within the sections, each chapter deals with an individual disease, opening with a useful summary of major phenotypic expression including clear and helpful biochemical pathways, identifying for the reader exactly where the defect occurs. Throughout the book, plentiful photographs, often showing extremely rare disorders, are an invaluable aid to diagnosis. Key Features • Fully updated to incorporate all new developments in the field • Brand new chapters cover methylmalonic aciduria of ACSF3 deficiency, branched chain keto acid dehydrogenase deficiency, serine deficiencies, purine nucleoside phosphorylase deficiency, antiquitin deficiency, and others • Excellent and detailed clinical descriptions, with numerous valuable hints and suggestions for management • Helpful explanatory algorithms and decision trees, and high-quality illustrative material including biochemical pathways and an unrivaled photographic collection, which enhance clinical applicability The fourth edition of this highly regarded book, authored by two of the foremost authorities in pediatric metabolic medicine, continues to provide incomparable insight into the problems associated with metabolic diseases and remains invaluable to pediatricians, geneticists, and general clinicians worldwide.

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871

Publisher

CRC Press

Published Date

ISBN 10

1138196606

ISBN 13

9781138196605

Pediatric Neurology Part III

Chapter 181. Defects in amino acid catabolism and the urea cycle

By: Georg F. Hoffmann,Stefan Kölker

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Pediatric Neurology Part III

Chapter 181. Defects in amino acid catabolism and the urea cycle

By: Georg F. Hoffmann,Stefan Kölker

Symptoms in patients with defects in amino acid catabolism and the urea cycle usually develop because of intoxication of accumulating metabolites. The cumulative prevalence of these disorders is considerable (at least>1:2000 newborns). Timely and correct intervention during the initial presentation and during later episodes is most important. Evaluation of metabolic parameters should be performed on an emergency basis in every patient with symptoms of unexplained metabolic crisis, intoxication, and/or unexplained encephalopathy. A substantial number of patients develop acute encephalopathy or chronic and fluctuating progressive neurological disease. The so-called cerebral organic acid disorders present with (progressive) neurological symptoms: ataxia, myoclonus, extrapyramidal symptoms, and “metabolic stroke.” Important diagnostic clues, such as white matter abnormalities, cortical or cerebellar atrophy, and injury of the basal ganglia can be derived from cranial magnetic resonance imaging (MRI). Long-term neurological disease is common, particularly in untreated patients, and the manifestations are varied, the most frequent being (1) mental defect, (2) epilepsy, and (3) movement disorders. Successful treatment strategies are becoming increasingly available. They mostly require an experienced interdisciplinary team including a neuropediatrician and/or later on a neurologist.

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Elsevier Inc. Chapters

Published Date

ISBN 10

0128084472

ISBN 13

9780128084472

Atlas of Inherited Metabolic Diseases 3E

By: William Nyhan,Georg Hoffmann,Bruce Barshop,Aida Al-Aqeel

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Atlas of Inherited Metabolic Diseases 3E

By: William Nyhan,Georg Hoffmann,Bruce Barshop,Aida Al-Aqeel

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889

Publisher

CRC Press

Published Date

ISBN 10

1444149482

ISBN 13

9781444149487

Book's by Georg F Hoffmann

The Encyclopaedia Logic, with the Zustze

The Encyclopaedia Logic, with the Zustze

Atlas of Inherited Metabolic Diseases

Atlas of Inherited Metabolic Diseases

Pediatric Neurology Part III

Pediatric Neurology Part III

Atlas of Inherited Metabolic Diseases 3E

Atlas of Inherited Metabolic Diseases 3E

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